Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 479127생성일: 2026년 10월 26일
2-Benzoylcyclohexanone → 2-(2-Benzoyl-phenylamino)-3-{4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-naphthalen-1-yl}-propionic acid ethyl ester
https://huagongshe.com/reaction/479127
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Benzoylcyclohexanone | HCID 275627 | — |
| 반응물 | 2-Amino-3-{4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-naphthalen-1-yl}-propionic acid ethyl ester | HCID 69557829 | — |
| 촉매 | Palladium | HCID 23938 | — |
| 용매 | Anisole | HCID 7519 | — |
| 생성물 | 2-(2-Benzoyl-phenylamino)-3-{4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-naphthalen-1-yl}-propionic acid ethyl ester | HCID 69557121 | 15.5% |
반응 단계
0.345 g of 2-Amino-3-{4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-naphthalen-1-yl}-propionic acid ethyl ester was dissolved in 6 ml of anisole and treated successively with 0.181 g (1.15 eq.) of 2-benzoyl-cyclohexanone and 60 mg of Pd/C (10%) and heated under Ar to 180-185° C. After 80 Min., additional 60 mg of fresh catalyst was added and heating continued for another 3.5 h. Cooling to RT, pouring onto crashed ice, twofold extraction with AcOEt, washing with water, drying over sodium sulfate, and purification by flash chromatography (SiO2, hexane/AcOEt 7/3) produced 0.075 g of the title compound in the less polar fractions and 0.285 g of intermediate enamine, which was processed once again as just described. Final purification left a combined crop of 0.221 g of 2-(2-benzoyl-phenylamino)-3-{4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-naphthalen-1-yl}-propionic acid ethyl ester as yellow, sticky oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06642389B2 |
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| 출처 데이터셋 | uspto-grants-2003_11 |
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| ORD ID | ord-5090fdba31e7417fbcbb4338bb908c19 |
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| 출처 메모 | uspto-grants-2003_11 |
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